STEREOSELECTIVE ADDITION OF ORGANOCOPPER REAGENTS TO ACETYLENIC ESTERS AND AMIDES - SYNTHESIS OF JUVENILE-HORMONE ANALOGS

被引：85

作者：

ANDERSON, RJ ^{[1
]}

CORBIN, VL ^{[1
]}

COTTERRELL, G ^{[1
]}

COX, GR ^{[1
]}

HENRICK, CA ^{[1
]}

SCHAUB, F ^{[1
]}

SIDDALL, JB ^{[1
]}

机构：

[1] ZOECON CORP,RES LAB,PALO ALTO,CA 94304

来源：

JOURNAL OF THE AMERICAN CHEMICAL SOCIETY | 1975年 / 97卷 / 05期

关键词：

D O I：

10.1021/ja00838a039

中图分类号：

O6 [化学];

学科分类号：

0703 ;

摘要：

引用

页码：1197 / 1204

页数：8

共 46 条

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[4] BOULARAN.G, 1967, B SOC CHIM FR, P1706
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[7] A CONVENIENT SYNTHESIS OF MIXED ISOMERS OF JUVENILE HORMONE
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[8] CONJUGATE ADDITIONS OF GRIGNARD REAGENTS TO ALPHA,BETA-UNSATURATED ESTERS .7. ADDITIONS TO ACETYLENIC ESTERS
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[9] MIXED CUPRATE REAGENTS OF TYPE R1R2CULI WHICH ALLOW SELECTIVE GROUP TRANSFER
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[J]. JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1972, 94 (20) : 7210 - &
[10] METHOD FOR STEREOSPECIFIC SYNTHESIS OF 1,3-DIENES AND 1,4-DIENES VIA ORGANOCOPPER REAGENTS
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